U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 1287

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 AGT, MAP10, 221 more genes
    nsv7148158copy number variation1nstd102humanPathogenic GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190 RNU6-747P, LINC01139, 172 more genes
    nsv7143593copy number variation1nstd232human GRCh37.p13 chr1: 239,895,948-239,896,102 , GRCh38.p12 chr1: 239,732,648-239,732,802 CHRM3
    nsv7099270copy number variation1nstd231human GRCh38.p12 chr1: 237,610,040-242,246,069 , GRCh37 chr1: 237,773,340-242,409,371 CHML, CHRM3, 59 more genes
    nsv7095603copy number variation1nstd102humanUncertain significance GRCh37 chr1: 240,070,603-240,072,524 , GRCh38.p12 chr1: 239,907,303-239,909,224 CHRM3
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7058034inversion1nstd229human GRCh38 chr1: 239,656,010-239,656,056 , GRCh37.p13 chr1: 239,819,310-239,819,356 CHRM3
    nsv7056472inversion1nstd229human GRCh38 chr1: 239,781,756-239,781,771 , GRCh37.p13 chr1: 239,945,056-239,945,071 CHRM3
    nsv7053843inversion1nstd229human GRCh38 chr1: 239,781,725-239,781,801 , GRCh37.p13 chr1: 239,945,025-239,945,101 CHRM3
    nsv7052616inversion1nstd229human GRCh38 chr1: 239,393,128-239,401,792 , GRCh37.p13 chr1: 239,556,428-239,565,092 CHRM3
    nsv7052196inversion1nstd229human GRCh38 chr1: 239,475,030-239,495,811 , GRCh37.p13 chr1: 239,638,330-239,659,111 CHRM3
    nsv7047070inversion1nstd229human GRCh38 chr1: 239,656,108-239,656,148 , GRCh37.p13 chr1: 239,819,408-239,819,448 CHRM3
    nsv7046870inversion1nstd229human GRCh38 chr1: 239,800,417-239,800,442 , GRCh37.p13 chr1: 239,963,717-239,963,742 CHRM3
    nsv7045904inversion1nstd229human GRCh38 chr1: 236,415,671-241,161,975 , GRCh37.p13 chr1: 236,578,971-241,325,275 PSMD2P1, RN7SKP195, 55 more genes
    nsv7045815inversion1nstd229human GRCh38 chr1: 239,463,740-239,470,202 , GRCh37.p13 chr1: 239,627,040-239,633,502 CHRM3
    nsv7044547inversion1nstd229human GRCh38 chr1: 234,053,817-240,091,334 , GRCh37.p13 chr1: 234,189,563-240,254,634 RNU6-725P, RNU6-968P, 101 more genes
    nsv7042685inversion1nstd229human GRCh38 chr1: 239,834,689-239,837,182 , GRCh37.p13 chr1: 239,997,989-240,000,482 CHRM3
    nsv7042632inversion1nstd229human GRCh38 chr1: 238,193,966-241,052,503 , GRCh37.p13 chr1: 238,357,266-241,215,803 LOC105373222, FMN2, 27 more genes
    nsv7041398inversion1nstd229human GRCh38 chr1: 239,472,902-239,480,056 , GRCh37.p13 chr1: 239,636,202-239,643,356 CHRM3
    nsv6677952copy number variation1nstd229human GRCh38 chr1: 239,531,420-239,538,727 , GRCh37.p13 chr1: 239,694,720-239,702,027 CHRM3
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center